The activation and functionalization of C–F bonds under mild conditions can serve as an
important tool for organic syntheses including the modification of pharmaceuticals and …

Photocatalyzed organic synthesis transformation is a remarkable green synthetic strategy
because of the advantages of operational simplicity, high chemoselectivities, cheap, and …

The sigma (σ)‐hole effect has emerged as a promising tool to construct novel architectures
endowed with new properties. A simple yet effective strategy for the generation of …

The difunctionalizative trifluoromethylation of unsaturated C− C bonds is a highly useful and
efficient method for the synthesis of trifluoromethyl compounds with attractive architectures …

The importance of fluorinated organic molecules in drugs and pharmaceuticals led to the
development of several synthetic methods for introducing fluorine into bioactive molecules …

Selective functionalization of C–F bonds in trifluoromethyl groups has recently received a
growing interest, as it offers atom-and step-economic pathways to access highly valuable …

The process of selectively introducing a CF 3 group into an organic molecule using
inexpensive, stable, and solid sodium trifluoromethanesulfinate has rapidly advanced in …

Conspectus Enamide and enecarbamate derivatives containing a nucleophilic center at the
β-position from their nitrogen atom as well as a latent electrophilic site at their α-position are …

The evaluation of the pentafluorocyclopropyl group as a chemotype in crop protection and
medicinal chemistry has been hampered in the past by the lack of suitable methodologies …

The use of visible light to promote synthetic processes has been emerging rapidly in recent
years. In the frame of eco-sustainable strategies involving the generation of reactive …